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963 total results
Comments (917)
@jesfactsmon Hi Hank and my fellow PN sufferes. I am coming off a very bad week...
https://connect.mayoclinic.org/comment/310971/
NOT have large fiber neuropathy or CIDP
@kevinversace55 If you haven’t had a neurologist test you with EMGs, nerve conduction studies, MRIs, MRNs...
https://connect.mayoclinic.org/comment/1049912/
I need to be tested for MS, CIDP, MSA
I had the positive test in early 2021 after symptoms of CIDP and the positive nerve...
https://connect.mayoclinic.org/comment/1047067/
test in early 2021 after symptoms of CIDP
Hi All, my story may or may not be of any note but here it is....
https://connect.mayoclinic.org/comment/876938/
Second neurologist said he had CIDP
I was only recently diagnosed with CIDP, but I have had it for over 13 years!!...
https://connect.mayoclinic.org/comment/859785/
I was only recently diagnosed with CIDP
Good morning, In response to your post, I have been receiving IgG infusions for over a...
https://connect.mayoclinic.org/comment/807547/
I was diagnosed with CIDP and I had
I had peripheral neuropathy develop after PMR was diagnosed. It slowly progressed its way up legs....
https://connect.mayoclinic.org/comment/1376028/
Demyelinating Polyradiculoneuropathy (CIDP
I gave Buprenorphine a try for over a year, hoping I could switch to that from...
https://connect.mayoclinic.org/comment/1028407/
't start with an opioid for my CIDP
I just happened on this discussion and have learned a lot about my own hammertoes. I...
https://connect.mayoclinic.org/comment/1021358/
Because of my CIDP, I'm pretty picky
Since I was diagnosed with sfpn or CIDP, I've seen neurologists, pain specialists, a pain therapist...
https://connect.mayoclinic.org/comment/966206/
Since I was diagnosed with sfpn or CIDP
My 72 yr. old husband had been a heavy drinker all his life. Maybe drank 2...
https://connect.mayoclinic.org/comment/913303/
#2 who said rare genetic disease, CIDP
@imagine1 Hello Dawn, I read your post and first I want to say I am sorry...
https://connect.mayoclinic.org/comment/872939/
experience with gabapentin, I have CIDP
@harley22 I have the same symptoms. My journey has been 12 years, too, but significant symptoms...
https://connect.mayoclinic.org/comment/1045773/
about if I get diagnosed with MS or CIDP
I’m a 75 yo lady with PN and balanci issues are a major problem as well...
https://connect.mayoclinic.org/comment/1240407/
have muscle atrophy and weakness from CIDP
That’s the problem I ran into. I got my questions answered and she wrote my doctors...
https://connect.mayoclinic.org/comment/1140506/
rheumatologist is starting me on IVIG for CIDP
I would be interested to know if your mom has any numbness in her toes, feet,...
https://connect.mayoclinic.org/comment/1092658/
I have CIDP, an autoimmune form of peripheral
I just joined Connect, and saw your post in another string about your post-infusion arm pain....
https://connect.mayoclinic.org/comment/81488/
I was diagnosed with CIDP in September
I also a very disappointed that Mayo isn’t taking any new neurology patients. I have been...
https://connect.mayoclinic.org/comment/1117638/
I have been diagnosed with CIDP as far
When I was diagnosed in late 2020, I was hospitalized by my Neurologist so that the...
https://connect.mayoclinic.org/comment/1049626/
Once CIDP was confirmed they blasted
Hi, everyone. I haven't done the AIP diet per se, but I'm looking into what anti-inflammatory...
https://connect.mayoclinic.org/comment/1044591/
inflammatory demyelinating polyneuropathy (CIDP
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